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LY3522348 is a highly selective, orally bioavailable small molecule inhibitor that targets human ketohexokinase isoforms C and A (hKHK-C, hKHK-A). It was developed to reduce the lipogenic effects of high fructose intake by inhibiting the enzyme responsible for fructose phosphorylation in the liver. This mechanism aims to decrease hepatic steatosis and fibrogenesis, making it a potential therapeutic candidate for metabolic diseases such as nonalcoholic steatohepatitis (NASH) and kidney disease. The drug has demonstrated robust pharmacodynamic responses in preclinical models of fructose metabolism and has advanced into clinical trials. LY3522348 was discovered and developed by Eli Lilly[1][2][4][5].
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